| pubmed-article:6322184 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C0014834 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C0008633 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C0085431 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C0598312 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C1704686 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C0439659 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C0037791 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
| pubmed-article:6322184 | lifeskim:mentions | umls-concept:C1710548 | lld:lifeskim |
| pubmed-article:6322184 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:6322184 | pubmed:dateCreated | 1984-4-24 | lld:pubmed |
| pubmed-article:6322184 | pubmed:abstractText | Escherichia coli rnh mutants defective in RNase H activity display the features of previously described sdrA (stable DNA replication) and dasF (dnaA suppressor) mutants: (i) sustained DNA replication in the absence of protein synthesis, (ii) lack of requirement for dnaA protein and the origin of replication (oriC), and (iii) sensitivity of growth to a rich medium. Both the sdrA mutants (selected for continued DNA replication in the absence of protein synthesis) and the dasF mutants (selected as dnaA suppressors) are defective in RNase H activity, measured in vitro. Furthermore, a 760-base-pair fragment containing the rnh+ structural gene complements the phenotype of each of the rnh, sdrA, and dasF mutants, indicative of a single gene. One function of RNase H in vivo is in the initiation of a cycle of DNA replication at oriC dependent on dnaA+. In keeping with these results, RNase H contributes to the specificity of dnaA protein-dependent replication initiated at oriC in a partially purified enzyme system. | lld:pubmed |
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| pubmed-article:6322184 | pubmed:language | eng | lld:pubmed |
| pubmed-article:6322184 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:6322184 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:6322184 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6322184 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:6322184 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:6322184 | pubmed:author | pubmed-author:OgawaTT | lld:pubmed |
| pubmed-article:6322184 | pubmed:author | pubmed-author:KornbergAA | lld:pubmed |
| pubmed-article:6322184 | pubmed:author | pubmed-author:KogomaTT | lld:pubmed |
| pubmed-article:6322184 | pubmed:author | pubmed-author:PickettG GGG | lld:pubmed |
| pubmed-article:6322184 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6322184 | pubmed:volume | 81 | lld:pubmed |
| pubmed-article:6322184 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6322184 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6322184 | pubmed:pagination | 1040-4 | lld:pubmed |
| pubmed-article:6322184 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:6322184 | pubmed:year | 1984 | lld:pubmed |
| pubmed-article:6322184 | pubmed:articleTitle | RNase H confers specificity in the dnaA-dependent initiation of replication at the unique origin of the Escherichia coli chromosome in vivo and in vitro. | lld:pubmed |
| pubmed-article:6322184 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:6322184 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:6322184 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:6322184 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:6322184 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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